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ST 1936 is a 5-HT(6) receptor agonist, which is a compound that interacts with the serotonin 5-HT(6) receptor. It has been proposed as a potential antidepressant and anti-anhedonic drug, making it a promising candidate for the treatment of psychiatric disorders such as depression.

1210-81-7

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1210-81-7 Usage

Uses

Used in Pharmaceutical Industry:
ST 1936 is used as a potential antidepressant and anti-anhedonic drug for the treatment of psychiatric disorders such as depression. It acts as a 5-HT(6) receptor agonist, which may help alleviate symptoms associated with these conditions.
Used in Research and Development:
ST 1936 is also used in research and development for the study of serotonin 5-HT(6) receptor agonists and antagonists, which can provide insights into the development of new treatments for psychiatric disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 1210-81-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,1 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1210-81:
(6*1)+(5*2)+(4*1)+(3*0)+(2*8)+(1*1)=37
37 % 10 = 7
So 1210-81-7 is a valid CAS Registry Number.

1210-81-7 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Sigma

  • (SML0260)  ST1936  ≥98% (HPLC)

  • 1210-81-7

  • SML0260-5MG

  • 803.79CNY

  • Detail
  • Sigma

  • (SML0260)  ST1936  ≥98% (HPLC)

  • 1210-81-7

  • SML0260-25MG

  • 3,261.96CNY

  • Detail

1210-81-7Upstream product

1210-81-7Downstream Products

1210-81-7Relevant academic research and scientific papers

PREPARATION OF 3-AMINOALKYL-SUBSTITUTED INDOLE DERIVATIVES FROM PHENYLHYDRAZINES AND AMINOKETONES

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Page 11, (2008/06/13)

The present invention relates to a process for the preparation of indole derivatives, particularly those, which are useful as pharmaceutical intermediates. The process involves formation of hydrazone derivative between a phenyl hydrazine and a ketone amine, followed by cyclisation to give desired 2,3-substituted indole derivative in the presence of acid catalyst.

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